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Marfan syndrome and pregnancy: maternal and neonatal outcomes
OBJECTIVE: To report outcomes in a recent series of pregnancies in women with Marfan syndrome (MFS). DESIGN: Retrospective case note review. SETTING: Tertiary referral unit (Chelsea and Westminster and Royal Brompton Hospitals). SAMPLE: Twenty-nine pregnancies in 21 women with MFS between 1995 and 2...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162995/ https://www.ncbi.nlm.nih.gov/pubmed/24418012 http://dx.doi.org/10.1111/1471-0528.12515 |
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author | Curry, RA Gelson, E Swan, L Dob, D Babu-Narayan, SV Gatzoulis, MA Steer, PJ Johnson, MR |
author_facet | Curry, RA Gelson, E Swan, L Dob, D Babu-Narayan, SV Gatzoulis, MA Steer, PJ Johnson, MR |
author_sort | Curry, RA |
collection | PubMed |
description | OBJECTIVE: To report outcomes in a recent series of pregnancies in women with Marfan syndrome (MFS). DESIGN: Retrospective case note review. SETTING: Tertiary referral unit (Chelsea and Westminster and Royal Brompton Hospitals). SAMPLE: Twenty-nine pregnancies in 21 women with MFS between 1995 and 2010. METHODS: Multidisciplinary review of case records. MAIN OUTCOME MEASURES: Maternal and neonatal mortality and morbidity of patients with MFS and healthy controls. RESULTS: There were no maternal deaths. Significant cardiac complications occurred in five pregnancies (17%): one woman experienced a type–A aortic dissection; two women required cardiac surgery within 6 months of delivery; and a further two women developed impaired left ventricular function during the pregnancy. Women with MFS were also more likely to have obstetric complications (OR 3.29, 95% CI 1.30–8.34), the most frequent of which was postpartum haemorrhage (OR 8.46, 95% CI 2.52–28.38). There were no perinatal deaths, although babies born to mothers with MFS were delivered significantly earlier than those born to the control group (median 39 versus 40 weeks of gestation, Mann–Whitney U–test, P = 0.04). These babies were also significantly more likely to be small for gestational age (24% in the MFS group versus 6% in the controls; OR 4.95, 95% CI 1.58–15.55). CONCLUSIONS: Pregnancy in women with MFS continues to be associated with significant rates of maternal, fetal, and neonatal complications. Effective pre-pregnancy counselling and meticulous surveillance during pregnancy, delivery, and the puerperium by an experienced multidisciplinary team are warranted for women with MFS. |
format | Online Article Text |
id | pubmed-4162995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41629952014-09-22 Marfan syndrome and pregnancy: maternal and neonatal outcomes Curry, RA Gelson, E Swan, L Dob, D Babu-Narayan, SV Gatzoulis, MA Steer, PJ Johnson, MR BJOG Maternal Medicine OBJECTIVE: To report outcomes in a recent series of pregnancies in women with Marfan syndrome (MFS). DESIGN: Retrospective case note review. SETTING: Tertiary referral unit (Chelsea and Westminster and Royal Brompton Hospitals). SAMPLE: Twenty-nine pregnancies in 21 women with MFS between 1995 and 2010. METHODS: Multidisciplinary review of case records. MAIN OUTCOME MEASURES: Maternal and neonatal mortality and morbidity of patients with MFS and healthy controls. RESULTS: There were no maternal deaths. Significant cardiac complications occurred in five pregnancies (17%): one woman experienced a type–A aortic dissection; two women required cardiac surgery within 6 months of delivery; and a further two women developed impaired left ventricular function during the pregnancy. Women with MFS were also more likely to have obstetric complications (OR 3.29, 95% CI 1.30–8.34), the most frequent of which was postpartum haemorrhage (OR 8.46, 95% CI 2.52–28.38). There were no perinatal deaths, although babies born to mothers with MFS were delivered significantly earlier than those born to the control group (median 39 versus 40 weeks of gestation, Mann–Whitney U–test, P = 0.04). These babies were also significantly more likely to be small for gestational age (24% in the MFS group versus 6% in the controls; OR 4.95, 95% CI 1.58–15.55). CONCLUSIONS: Pregnancy in women with MFS continues to be associated with significant rates of maternal, fetal, and neonatal complications. Effective pre-pregnancy counselling and meticulous surveillance during pregnancy, delivery, and the puerperium by an experienced multidisciplinary team are warranted for women with MFS. Blackwell Publishing Ltd 2014-04 2014-01-13 /pmc/articles/PMC4162995/ /pubmed/24418012 http://dx.doi.org/10.1111/1471-0528.12515 Text en © 2014 The Authors BJOG An International Journal of Obstetrics and Gynaecology published by John Wiley & Sons Ltd on behalf of Royal College of Obstetricians and Gynaecologists http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open access article under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made. |
spellingShingle | Maternal Medicine Curry, RA Gelson, E Swan, L Dob, D Babu-Narayan, SV Gatzoulis, MA Steer, PJ Johnson, MR Marfan syndrome and pregnancy: maternal and neonatal outcomes |
title | Marfan syndrome and pregnancy: maternal and neonatal outcomes |
title_full | Marfan syndrome and pregnancy: maternal and neonatal outcomes |
title_fullStr | Marfan syndrome and pregnancy: maternal and neonatal outcomes |
title_full_unstemmed | Marfan syndrome and pregnancy: maternal and neonatal outcomes |
title_short | Marfan syndrome and pregnancy: maternal and neonatal outcomes |
title_sort | marfan syndrome and pregnancy: maternal and neonatal outcomes |
topic | Maternal Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4162995/ https://www.ncbi.nlm.nih.gov/pubmed/24418012 http://dx.doi.org/10.1111/1471-0528.12515 |
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